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Water-soluble azo compound or salt thereof, ink and recording medium

A compound, hydrophilic group technology, applied in the field of recording media to which the water-soluble azo compound or its salt or ink is attached, can solve problems such as poor fastness

Active Publication Date: 2019-06-14
NIPPON KAYAKU CO LTD
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

However, the fastness of recorded images such as light fastness is inferior to that of pigments

Method used

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  • Water-soluble azo compound or salt thereof, ink and recording medium
  • Water-soluble azo compound or salt thereof, ink and recording medium
  • Water-soluble azo compound or salt thereof, ink and recording medium

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0404] (Process 1)

[0405] While dissolving 20.8 parts of 5-amino-2-chlorobenzenesulfonic acid in 200 parts of water, adjust the pH to 6 with sodium hydroxide, and then add 7.2 parts of sodium nitrite. This solution was added dropwise to 200 parts of 5% hydrochloric acid at 0°C to 10°C for 30 minutes, and then stirred at 10°C or less for 1 hour to perform diazotization reaction to prepare a diazonium reaction liquid.

[0406] On the other hand, 26.6 parts of 2-(sulfopropoxy)-5-chloroaniline was dissolved in 130 parts of water while the pH was adjusted to 7 with sodium hydroxide, 10.4 parts of sodium bisulfite and 8.6 parts of 35% fu Ermarin, methyl-ω-sulfonic acid derivatives were prepared by conventional methods. The obtained methyl-ω-sulfonic acid derivative was added to the previously prepared diazonium reaction solution, and stirred for 24 hours under the conditions of 0°C to 15°C and pH 2 to pH4. After adjusting the reaction solution to pH 11 with sodium hydroxide, it was s...

Embodiment 2

[0414] In Example 1 (Step 2), except that 5.3 parts of DL-2-amino-1-butanol was used instead of 6.2 parts of 4-amino-2-methyl-1-butanol, the same as in Example 1 was obtained to obtain 11.3 parts of the sodium salt (λmax: 418.4 nm) of the compound of the present invention represented by the following formula (102) were used.

[0415] [Chemical formula 30]

[0416]

[0417] [Preparation of Ink]

[0418] The components shown in Table 47 below were mixed to obtain a solution, and after that, the inks of Example 1, Example 2, and Comparative Example 1, and Comparative Example 2 were prepared by precision filtration using a 0.45 μm membrane filter. The value in the table means "parts", and "-" means that the ingredient is not included.

[0419] In the following table 47, "aq.NaOH (NaOH aqueous solution)" is the "remaining part" means adding 25% sodium hydroxide aqueous solution and water to the mixed solution of each component to adjust the pH of each solution to 8.0 To 9.5, and adjust t...

Embodiment 3

[0451] In Example 1 (Step 2), except that 4.5 parts of 2-(methylamino)ethanol was used instead of 6.2 parts of 4-amino-2-methyl-1-butanol, it was the same as Example 1, and 11.2 was obtained. Part of the sodium salt (λmax: 418.5 nm) of the compound of the present invention represented by the following formula (103).

[0452] [Chemical formula 32]

[0453]

[0454] [Preparation of Ink]

[0455] The ink of Example 3 was prepared in the same manner as in Example 1, except that the compound represented by the above formula (103) was used instead of the compound represented by the above formula (101).

[0456] [Inkjet Recording]

[0457] Using an inkjet printer (manufactured by Canon Co., Ltd., trade name: PIXUS ip 7230), various inks of Example 3 and the above-mentioned Comparative Example 1 and Comparative Example 2 were attached to the following glossy paper 1 to glossy paper 4, and performed Inkjet recording. During recording, an image pattern was made in a manner of obtaining six lev...

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Abstract

Provided are a compound represented by formula (1) or a salt thereof, and an ink comprising the same. In formula (1): Q's independently represent a halogen atom; R11 and R12 independently represent analkyl group substituted by an ionic hydrophilic group; and A1 represents a C1-C3 alkoxy-substituted alkylamino group, etc.

Description

Technical field [0001] The present invention relates to a water-soluble azo compound or its salt, an ink containing the water-soluble azo compound or its salt, an inkjet recording method using the ink, an inkjet printer filled with a container containing the ink, and Water-soluble azo compound or its salt or ink recording medium. Background technique [0002] Among various color recording methods, a recording method using an inkjet printer, which is one of its representative methods, has developed various ink ejection methods. These ejection methods all make ink droplets and attach them to various recording media (paper, film, cloth, etc.) for recording. In this method, since the recording head and the recording medium are not in direct contact with each other, no sound is produced and it is very quiet. In addition, due to its features such as easy miniaturization, high speed, and colorization, this method has rapidly spread in recent years and is expected to grow substantially...

Claims

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Application Information

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Patent Type & Authority Applications(China)
IPC IPC(8): C09B43/16B41J2/01B41M5/00C09D11/328
CPCC09B43/16C09D11/328C09D11/36B41M5/0023B41M5/50B41J2/17503B41M5/502C07D251/70C07D405/12C09D11/033C09D11/037
Inventor 永塚真也饭野拓武藤瞳
Owner NIPPON KAYAKU CO LTD